Variant #0000515467 (NC_000002.11:g.26414235C>T, NM_000182.4:c.2176G>A (HADHA))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.26414235C>T
DNA change (hg38) g.26191366C>T
Published as HADHA(NM_000182.5):c.2176G>A (p.A726T)
ISCN -
DB-ID HADHA_000010
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HADHA NM_000182.4 ?/. - c.2176G>A r.(?) p.(Ala726Thr)
HADHB NM_000183.2 ?/. - c.-53632C>T r.(?) p.(=)


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